Diclofex DC
- Product NDC
- 51021-372
- 11-digit product format
- 510210372
- Labeler code
- 51021
- Product ID
- 51021-372_073f47e3-0e56-48c3-85af-baba7a4826dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium and Capsaicin
- Dosage form
- KIT
- Labeler
- Sircle Laboratories, LLC
- Application
- ANDA204132
- Marketing category
- ANDA
- Marketing start
- 2016-04-30
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51021-372-01 | ML - Milliliter | 51021-372 | 23cf166b-8103-41ba-be75-850ce1f40c48 | 1 | 2017-11-06 |